Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000200513 | SCV000253366 | benign | Pancreatic adenocarcinoma | 2023-08-04 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV004717085 | SCV005303937 | benign | not provided | criteria provided, single submitter | not provided | ||
Prevention |
RCV003927853 | SCV004747009 | likely benign | PALLD-related disorder | 2021-11-01 | no assertion criteria provided | clinical testing | This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |